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In one study, the prevalence of this polymorphism was found to be higher than in controls in the parents of NTD fetuses and in the fetuses themselves: homozygosity for the TT mutation was found in 13% of cases compared with 5% of control subjects

Ongoing research aims to understand how these peptides might affect neurotransmitter levels, neuroprotection, and cellular regeneration

D55.x Anemia Due to Enzyme Disorders These include rare conditions like G6PD deficiency

One unprotected afternoon outside can trigger hyperpigmentation that takes months to fade

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BMC Genomics 16:S5